Recurrence of Split Hand/Foot Malformation, Cleft Lip/Palate, and Severe Urogenital Abnormalities due to Germline Mosaicism for TP63 Mutation

被引:7
|
作者
Enriquez, Annabelle [1 ,2 ]
Krivanek, Michael [3 ]
Floettmann, Ricarda [4 ]
Peters, Hartmut [4 ]
Wilson, Meredith [1 ,2 ]
机构
[1] Childrens Hosp Westmead, Dept Clin Genet, Locked Bag 4001, Westmead, NSW 2145, Australia
[2] Univ Sydney, Discipline Genet Med, Sydney, NSW, Australia
[3] Childrens Hosp Westmead, Dept Histopathol, Westmead, NSW, Australia
[4] Charite Univ Med Berlin, Inst Med Genet & Human Genet, Berlin, Germany
关键词
TP63; congenital limb deformities; split hand/foot malformation; cleft lip; cleft palate; ectodermal dysplasia; urogenital abnormalities; germline mosaicism; GENOTYPE-PHENOTYPE CORRELATION; P63; GENE-MUTATIONS; EEC-SYNDROME; ECTODERMAL DYSPLASIA; ADULT-SYNDROME; P53; HOMOLOG; LIP-PALATE; ANOMALIES; DEFECTS; LIMB;
D O I
10.1002/ajmg.a.37816
中图分类号
Q3 [遗传学];
学科分类号
071007 ; 090102 ;
摘要
We describe two sibling fetuses with urogenital abnormalities detected by prenatal ultrasound, in which post-delivery examination showed split hand and foot malformation, and bilateral cleft lip and palate. These findings are consistent with ectrodactyly-ectodermal dysplasia-cleft lip with or without cleft palate syndrome (EEC). Both fetuses were found to have the same missense mutation in TP63 (c.1051G > A; p.D351N). Parental clinical examinations and lymphocyte DNA analyses were normal. This report illustrates the potential severity of urogenital defects in TP63-related disorders, which may be detectable with fetal ultrasonography. It highlights the need to counsel for the possibility of germline mosaicism in TP63-associated disorders. (C) 2016 Wiley Periodicals, Inc.
引用
收藏
页码:2372 / 2376
页数:5
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